(Q28024615)
English
autosomal recessive nonsyndromic deafness 3
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the MYO15A gene on chromosome 17p11
- DFNB3
- NRSD3
- autosomal recessive deafness 3, neurosensory nonsyndromic recessive deafness 3
- Deafness, Autosomal Recessive type 3
- DEAFNESS, AUTOSOMAL RECESSIVE 3; DFNB3
- DEAFNESS, AUTOSOMAL RECESSIVE 3
- Neurosensory Nonsyndromic Recessive Deafness 3
- autosomal recessive nonsyndromic deafness type 3
Statements
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Identifiers
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